BIOL 273 - Unit 3.3 Flashcards

1
Q

What happens to A band during muscle contraction

A

remains constant - therefore myosin shortening could not be responsible for muscle contraction

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2
Q

Describe the sliding filament theory

A
  • At rest the ends of thick (myosin) and thin (actin) filaments overlap slightly within each sarcomere
  • Thick and thin filaments slide past each other with no change in the length of the filaments themselves
  • The thin (actin) filaments slide along the thick (myosin) filaments towards the M line of the sarcomere - brings the Z disks closer together
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3
Q

What happens to the H zone during the sliding filament theory

A

decreases

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4
Q

What happens to the A band during sliding filament theory

A

remains constant

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5
Q

What happens to the Z discs during the sliding filament theory

A

closer to M line

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6
Q

What happens to the I band during the sliding filament theory

A

decrease

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7
Q

What do skeletal muscles need to be stimulated by to contract

A

somatic motor neuron from the nervous system

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8
Q

What is released by the neuron into the synaptic cleft at the neuromuscular junction, what does this neurotransmitter bind to?

A
  • ACh released
  • binds to nicotinic cholinergic receptors on highly folded muscle motor end plates (aka Na+/K+ channels)
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9
Q

What happens when ACh binds to Na+/K+ channels

A
  • allows Na+ and K+ to move across the membrane
  • ACh is removed by acetylcholinesterase
  • Na+ influx exceeds K+ efflux
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10
Q

What happens when Na+ influx exeeds K+ efflux , what is it called

A

local depolarization occurs at the synapse
- called End Plate Potential - EPP

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11
Q

What happens during depolarization , EPP, what structure does it interact with

A

the potential moves down the T-tubule system
- T tubule membrane contains dihydropyridine (DHP receptors) - L type calcium channel

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12
Q

What happens on the T-tubule membrane when it is depolarized

A
  • DHP receptors changes conformation
  • they are mechanically linked to Ca 2+ channels of the SR called ryanodine receptors (RyR)
  • RyR changes conformation whih allows for opening of SR Ca+2 channels (calcium leaves the SR)
  • increasing cytosolic Ca2+
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13
Q

What happens when calcium is roaming free in the cytosol

A

Ca+2 binds to troponin on the thin filament
- this moves tropomyosin into the “on” position revealing actin binding sites

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14
Q

the binding of calcium and acting on regulatory proteins on thin filament results in what process

A

the crossbridge cycle

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15
Q

What is myosin’s function in the crossbridge theory

A

converting chemical energy (ATP) into movement

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16
Q

What are the binding sites of myosin

A

actin and ATP

17
Q

When does myosin bind to actin during the crossbridge cycle

A

when actin is exposed when Ca2+ binds to troponin
- this forms the crossbridge

18
Q

What happens when the myosin heads binds to actin during crossbridge cycle , what is this process called

A

inorganic phosphate releases from myosin (1st)
- causes myosin head to pivot toward the centre of the sarcomere
- called the powerstroke
- pulls thin filament towards the M line
- followed by the released of ADP from myosin (2nd)

19
Q

When does the myosin head (crossbridge) detach

A

when a new molecule of ATP attaches to the myosin head

20
Q

When does the myosin head return to the cocked position

A

when the myosin head ATPase hydrolyses ATP to ADP and Pi

21
Q

When does relaxation of the skeletal muscle occur

A

When Ca2+ is pumped back into SR through the Ca2+ ATPase (against concentration gradient)
- decrease in calcium in cytosol causes troponin and calcium to unbind

  • troponin shift to too position and covers binding site on actin of thin filament
22
Q

When does Glycolysis occur , what does it produce

A

in the presence or absence of oxygen
- provides limited amount of ATP - 2
- produces lactic acid

23
Q

Creatine phosphate

A

high energy phosphate molecule
- highly concentrated in muscles , provides a rapid source of energy
- easily donates inorganic phosphate to ADP to create ATP (provides a limited supply of ATP)

24
Q

Purpose of creatine phosphate

A

buffer concenration of ATP over very short time
creatine + ADP to ATP + creatine
(catalyzed by creatine kinase)

25
Twitch in muscle contraction
a single contraction-relaxation cycle (dependant on the movement of calcium to and from SR)
26
Latent period in muscle contraction
short delay between the AP and the beginning of the muscle tension excitation and contraction coupling <- the time it takes for that to occur - ends when calcium is binded to troponin to develop tension
27
What are the three types of muscle fibres
1. Slow-twitch fibres (type I) 2. Fast-twitch oxidative-glycolytic fibres (type IIA) 3. Fast-twitch glycolytic fibres (type IIX) depends on the primary source of energy (glycolysis or oxidation)
28
Oxidative fibres
- dark red in appearance due to myoglobin - Myoglobin -> an oxygen carrying haeme protein - predominantly produce ATP via oxidative metabolism - diamater of cell is smaller , numerous mitochondria , many capillaries (vascularized)
29
Fast or slow fibres
- refers to the rate of myosin hydrolize ATP and undergo crossbridge cycle Fast fibres: split ATP more quickly / crossbridge cycle & tension faster - result of the presence of different isoforms of myosin
30
Short twitch duration is useful for what
rapid, small muscle contractions (playing the piano)
31
Long twitch duration is good for what
long sustained movements (lifting heavy loads)
32
Twitch duration is determined by what
by the rate of removal of calcium ions from the cytosol
33
Which muscle has highest rate of removal from cytosol
fast twitch muscles - includes the contraction AND relaxation